Canonical Allele Identifier: PA2825517046
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 2077841
ClinVar RCV Id: RCV002985730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077430.1:p.Pro1409Leu
CA9396508
NM_001083961.2:c.4226C>T